Examples of 'thioethers' in a sentence
Meaning of "thioethers"
Thioethers - (noun) a class of organic compounds containing a sulfur atom bonded to two alkyl oraryl groups
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- plural of thioether
How to use "thioethers" in a sentence
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thioethers
It oxidizes thioethers to sulfoxides and organometallic complexes.
Thiols are readily alkylated to give thioethers.
Thioethers can be made vía the same procedure.
This odor limits the applications of volatile thioethers.
Thioethers are the sulfur analogs of ethers.
This category excludes thioethers.
Thioethers are also highly susceptible to oxidation.
Pharmaceutical use of aromatic thioethers.
Insecticidal thioethers and derivatives thereof.
A number of xanthates were successfully transformed into the corresponding aryl thioethers.
In thiol and thioethers the conformational preference is not so marked.
The above reaction with cyanogen bromide allows thioethers to be cleaved.
Preferred additives are thioethers of dibenzylidene sorbitol such as alkylthiodibenzylidene sorbitols.
Still another component is selected from the group consisting of thioethers.
Thioethers may also be used.
See also
Preferred additives are thioethers.
The required thioethers can be prepared easily by exchange with a thiol.
Sulfonium compounds are usually synthesized by the reaction of thioethers with alkyl halides.
Thiols and thioethers are the sulfur analogues of alcohols and ethers.
The method is also suitable in the deprotection of allyl esters and thioethers.
More recently crown thioethers have been suggested for use as ripening agents.
The present invention relates to a process for preparing biphenyl type aromatic thioethers.
Some thioethers are named by modifying the common name for the corresponding ether.
The above reaction with cyanogen bromide makes it possible to cleave the thioethers.
Lactone compounds and cyclic thioethers as well as vinyl thioethers can also be used.
Other examples of suitable higher temperature antioxidants are the thioethers and polymers thereof.
Thioethers In can also be formed under similar conditions.
There are two well known processes for preparing hydroxyalkylphenyl ethers and thioethers.
Thiols and Thioethers.
Thiol groups may also be reacted with epoxides in aqueous solution to yield hydroxy thioethers.
Thioethers are typically prepared by the alkylation of thiols,.
Chemicals or metabolites in human specimens Mutagenicity in urine Thioethers in urine.
Then, oxidation of thioethers was performed to synthesize sulfones.
Scheme B illustrates an alternative method for preparing substituted phenolic thioethers of this invention.
Also, thioethers such as tetrahydrothiophene can be used.
Scheme A illustrates a general method for preparing substituted phenolic thioethers of this invention.
For example, it converts thioethers into sulfoxides and sulfones.
It adds to alkenes to give chloride-substituted thioethers.
Thioethers are characterized by their strong odors, which are similar to thiol odor.
Petroleum contains many organosulfur compounds, including thioethers.
Thioethers, methods for their preparation, and compositions including such thioethers.
Isocynanate-capped variants of these thioethers are also included.
As indicated, certain embodiments of the present invention are directed to thioethers.
Examples of thioethers include, but are not limited to alkthioalkyls, alkthioalkenyls and alkthioalkynyls.
Other linking groups are ethers, thioethers and amines.
It is, therefore, a primary object of the present invention to provide novel substituted phenolic thioethers.
Simple organosulfur compounds such as thiols and thioethers are unreactive, however.
Thioethers are important in biology, notably in the amino acid methionine and the cofactor biotin.
In certain respects, the present invention is directed to thioethers.
Amides, ethers and thioethers are representative of couples which may be used for this purpose.
